The UMD-APC mutations database
Record ID: 2970

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.667C>Tp.Gln223X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnTAAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
 NoNo

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Patient and sample data


Sample IDPatient status
19_23086---23086-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data